http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#head http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#assertion http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#provenance http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#assertion http://rdf.disgenet.org/resource/gda/DGNcb476538bf4c5d64f4eb70e9933d9374 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/10249 http://rdf.disgenet.org/resource/gda/DGNcb476538bf4c5d64f4eb70e9933d9374 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0001418 http://rdf.disgenet.org/resource/gda/DGNcb476538bf4c5d64f4eb70e9933d9374 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#provenance http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#assertion http://purl.org/dc/terms/description [Although GTT mutation in codon 12 was predominantly observed in adenocarcinoma (10 of 11), GAT mutation (12 of 33) was as frequent as GTT mutation (11 of 33) in ACF together with mutation at codon 13 (7 of 33).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#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/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/7889486 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#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/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/dc/terms/created 2017-10-17T13:17:54+02:00 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1210536.RALdPT0eEvWV8QzRFag7a0h3JRtv5S_4eIQZeyYhXB5YM 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