Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_assertion description "[Compared to PLEKHA1, HTRA1/LOC387715 genetic variations were independently and strongly associated with exudative AMD in the French population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_assertion evidence source_evidence_literature NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_assertion SIO_000772 18079691 NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_assertion wasDerivedFrom befree-2016 NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_assertion wasGeneratedBy ECO_0000203 NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.
- befree-2016 importedOn "2016-02-19" NP645209.RA94mT8I3mXjDDeEYjB9P1QAXFjfT13b6Dru0w4dfFUlc130_provenance.