Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_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." NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_assertion evidence source_evidence_literature NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_assertion SIO_000772 15293282 NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_assertion wasDerivedFrom gad-20130706 NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_assertion wasGeneratedBy ECO_0000203 NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88208.RANp8_miXnRvo2klY9tl44v8fKzGJDFQBPmeS0LqfzjxA130_provenance.