http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#head
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#assertion
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#provenance
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#assertion
http://rdf.disgenet.org/resource/gda/DGN2b7e7a3241617e28832e250cecbc7e30
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/5554
http://rdf.disgenet.org/resource/gda/DGN2b7e7a3241617e28832e250cecbc7e30
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0398623
http://rdf.disgenet.org/resource/gda/DGN2b7e7a3241617e28832e250cecbc7e30
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#provenance
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#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/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#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/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/12172465
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#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/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/dc/terms/created
2017-10-17T13:15:36+02:00
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP849837.RAWn4hsfYxWtVkDPACxm_TUdQb80FR7c9kXC8V_sI1mGk
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