Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_assertion description "[Germline NF1, c-RET, SDH, and VHL mutations cause familial pheochromocytoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_assertion evidence source_evidence_literature NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_assertion SIO_000772 16098468 NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_assertion wasDerivedFrom befree-20140225 NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_assertion wasGeneratedBy ECO_0000203 NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP652912.RAPzdePAq6Aye20_8jDgfHKq60-y59j18jSw3SQHbhJc4130_provenance.