http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#head http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#assertion http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#provenance http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#assertion http://rdf.disgenet.org/resource/gda/DGN4e7b612ca15cc93bd7766048de5162ce http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/1287 http://rdf.disgenet.org/resource/gda/DGN4e7b612ca15cc93bd7766048de5162ce http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1567741 http://rdf.disgenet.org/resource/gda/DGN4e7b612ca15cc93bd7766048de5162ce http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#provenance http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#assertion http://purl.org/dc/terms/description [Recent genetic studies indicate that Alport syndrome and thin glomerular basement membrane disease (TMD) may both be due to COL4A3, COL4A4, and COL4A5 mutations, but there is continuing uncertainty concerning the diagnosis and management of patients without classic family history and symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#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/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/12203217 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#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/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/dc/terms/created 2017-10-17T13:11:39+02:00 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP228209.RAF4c9thNl8mo3gMvcycWsb2Dhgn7jCVcj1u_hAwdtn-4 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