Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_assertion description "[We have now identified 13 ABCA1 mutations in 11 families (five TD, six FHA) and have examined the phenotypes of 77 individuals heterozygous for mutations in the ABCA1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_assertion evidence source_evidence_literature NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_assertion SIO_000772 11086027 NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_assertion wasDerivedFrom befree-20140225 NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_assertion wasGeneratedBy ECO_0000203 NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401023.RAlbTaFwTGrOG_-Qh8hwYnImmbSG6SIJw37rGJJwkBQCw130_provenance.