Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_assertion description "[We therefore determine in this study the relative frequency of mutations in PLCE1, WT1 or LAMB2 as the cause of IDMS in a worldwide cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_assertion evidence source_evidence_literature NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_assertion SIO_000772 18065803 NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_assertion wasDerivedFrom befree-20150227 NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_assertion wasGeneratedBy ECO_0000203 NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP958125.RApRYVvYTepGLLHc9FdDSDern8PSlx77m7E8Ww6KqVSCI130_provenance.