Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_assertion description "[Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_assertion evidence source_evidence_literature NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_assertion SIO_000772 11978965 NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_assertion wasDerivedFrom befree-20140225 NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_assertion wasGeneratedBy ECO_0000203 NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658090.RAF5oTq4RK0M8Ys0Wcq7UWc6fBNpPEzF2AqXIxphbOY6s130_provenance.