http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#head http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#assertion http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#provenance http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#assertion http://rdf.disgenet.org/resource/gda/DGNeb677cbe37e2c2461433305db210bf3d http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4524 http://rdf.disgenet.org/resource/gda/DGNeb677cbe37e2c2461433305db210bf3d http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0027794 http://rdf.disgenet.org/resource/gda/DGNeb677cbe37e2c2461433305db210bf3d http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#provenance http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#assertion http://purl.org/dc/terms/description [Methylenetetrahydrofolate reductase (MTHFR) mutations are commonly associated with hyperhomocysteinemia, and, through their defects in homocysteine metabolism, they have been implicated as risk factors for neural tube defects and unexplained, recurrent embryo losses in early pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#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/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/10958762 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#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/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/dc/terms/created 2017-10-17T13:14:46+02:00 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP719618.RAkYTznMRLIk-sOSi6tQMTS3a7JcUcmcFd_ZoFH7nrb0o 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