Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_assertion description "[Mutation analysis using sequencing of RT-PCR products and Northern blot analysis in MKS patients exclude PNUTL2 as the gene for MKS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_assertion evidence source_evidence_literature NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_assertion SIO_000772 9889007 NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_assertion wasDerivedFrom befree-2016 NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_assertion wasGeneratedBy ECO_0000203 NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1412725.RA3i7sTG_pmpAIAwnz7_1utK_LHQhlhvidrKZKRX58q2Y130_provenance.