Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_assertion description "[The factor V G1691A mutation is a risk for porencephaly: A case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_assertion evidence source_evidence_literature NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_assertion SIO_000772 15293282 NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_assertion wasDerivedFrom gad-20150221 NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_assertion wasGeneratedBy ECO_0000203 NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP141268.RAfgCgAmSUbqsOnynh7TSPbovPX3TPnYyZxD7iW9YtDzE130_provenance.