Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_assertion description "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_assertion evidence source_evidence_literature NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_assertion SIO_000772 16211558 NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_assertion wasDerivedFrom gad-20150221 NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_assertion wasGeneratedBy ECO_0000203 NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.