Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_assertion description "[Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_assertion evidence source_evidence_curated NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_assertion SIO_000772 25401301 NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_assertion wasDerivedFrom ctd_human-20150221 NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_assertion wasGeneratedBy ECO_0000218 NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP11102.RAjxspymUpDeMUiC5UVk_0VD-a6D5HMWH1Y51M_dP1byI130_provenance.