Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_assertion description "[One paraganglioma with no known SDH mutation but clinical features suggesting familial disease was negative, and one showed weak diffuse staining.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_assertion evidence source_evidence_literature NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_assertion SIO_000772 20236688 NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_assertion wasDerivedFrom befree-20150227 NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_assertion wasGeneratedBy ECO_0000203 NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP858126.RAfsoPK-AoFBaT6WVZ_5sR4hSHl_ZC0n7QwcKogmYQKgk130_provenance.