Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_assertion description "[SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_assertion evidence source_evidence_literature NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_assertion SIO_000772 15088139 NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_assertion wasDerivedFrom befree-20140225 NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_assertion wasGeneratedBy ECO_0000203 NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP543718.RAxHx05ktqzO62zsQKFlyi0uLvo4TflCptj1wuirsa2lk130_provenance.