Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_assertion description "[However, she had no mutations in FHBL candidate genes (APOB, PCSK9 and ANGPTL3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_assertion evidence source_evidence_literature NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_assertion SIO_000772 23043934 NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_assertion wasDerivedFrom befree-20150227 NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_assertion wasGeneratedBy ECO_0000203 NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP889511.RAFUSXVzQ3iUJ_WSHmDApYgQQajP-7X_cJTHqWU0x5KEY130_provenance.