Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_assertion description "[Sequencing of MYH11 revealed an in frame splice-site alteration in one out of two probands with TAA(D) associated with PDA but none in the series of 22 probands from the cohort of 110 patients with non-syndromic TAAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_assertion evidence source_evidence_literature NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_assertion SIO_000772 21937134 NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_assertion wasDerivedFrom befree-20140225 NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_assertion wasGeneratedBy ECO_0000203 NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP849870.RATW1HssIlPTzDFBfvyRL2PyG4HT_OKLlHIYSpUN3XPAI130_provenance.