Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_assertion description "[Cluster 1 PGLs exhibit VHL and/or succinate dehydrogenase (SDH) mutations and a pseudohypoxic phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_assertion evidence source_evidence_literature NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_assertion SIO_000772 21422080 NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_assertion wasDerivedFrom befree-2016 NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_assertion wasGeneratedBy ECO_0000203 NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.
- befree-2016 importedOn "2016-02-19" NP881006.RAxlnJpRYhS2xV2WybvxKQeSyE3VRrSZ197fIe9unDV_A130_provenance.