Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_assertion description "[When the mutation is located on chromosome 16 (PKD1), extra-renal manifestations such as the rupture of intracranial aneurysms are well known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_assertion evidence source_evidence_literature NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_assertion SIO_000772 8749697 NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_assertion wasDerivedFrom befree-20150227 NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_assertion wasGeneratedBy ECO_0000203 NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626632.RAT0pZrmgP-M1SbhrCAG-q3cskFyVupGGtSO1FStzOR6w130_provenance.