http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#head http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#assertion http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#provenance http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#assertion http://rdf.disgenet.org/resource/gda/DGNdf0626bb5d0e7de8d8802e0cc62037c4 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4143 http://rdf.disgenet.org/resource/gda/DGNdf0626bb5d0e7de8d8802e0cc62037c4 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C4048705 http://rdf.disgenet.org/resource/gda/DGNdf0626bb5d0e7de8d8802e0cc62037c4 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#provenance http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#assertion http://purl.org/dc/terms/description [Individuals, with hypermethioninemia due to one of the MAT1A mutations that in heterozygotes cause relatively mild and clinically benign hypermethioninemia are currently often being flagged in screening programs measuring methionine elevation to identify newborns with defective cystathionine ?-synthase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#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/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/26289392 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#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/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/dc/terms/created 2017-10-17T13:14:26+02:00 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP667075.RANlVlRTKERRBJLRHtrcJjUJhLW-XONawynvNsnXJ1CSY 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