http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#head http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#assertion http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#provenance http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#assertion http://rdf.disgenet.org/resource/gda/DGN018c93b7a20c0ccc1770da0d29ba0a0d http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5340 http://rdf.disgenet.org/resource/gda/DGN018c93b7a20c0ccc1770da0d29ba0a0d http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0398623 http://rdf.disgenet.org/resource/gda/DGN018c93b7a20c0ccc1770da0d29ba0a0d http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#provenance http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#assertion http://purl.org/dc/terms/description [After confirming clinically suspected thromboembolism with suitable imaging methods, pediatric patients should be screened for common gene mutations (factor V G1691A, prothrombin G20210A and MTHFR C677T genotypes), rare genetic deficiencies (protein C, protein S, antithrombin, and plasminogen), and new candidates for genetic thrombophilia causing elevated levels of lipoprotein(a), and homocysteine, and probable genetic risk factors (elevations in fibrinogen, factor IX, and factor VIIIC, and decreases in factor XII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/12172465 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/dc/terms/created 2017-10-17T13:15:29+02:00 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP830908.RADUanmvTjihf0f7de_aMI_10Bqy-Fz0GpmcbRmGqbLto http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0