Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_assertion description "[A novel missense SNRNP200 mutation associated with autosomal dominant retinitis pigmentosa in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_assertion evidence source_evidence_literature NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_assertion SIO_000772 23029027 NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_assertion wasDerivedFrom befree-20150227 NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_assertion wasGeneratedBy ECO_0000203 NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP866987.RAHQfI5vxwnb1ispP1QBn5Hkw28xxnLjgilHT2BzR_azo130_provenance.