Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_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." NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_assertion evidence source_evidence_literature NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_assertion SIO_000772 11086027 NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_assertion wasDerivedFrom befree-2016 NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_assertion wasGeneratedBy ECO_0000203 NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.
- befree-2016 importedOn "2016-02-19" NP300970.RAXiUVR9h9sCPVeX6CbezOHfRrMsQjR7WTRBzfwX-EgW4130_provenance.