Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion description "[This mutation, in a non-collagenous interruption associated with severe renal disease, provides evidence for the importance of this structural motif and suggests the range of phenotypes associated with COL4A5 mutations is more diverse than previously realized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion evidence source_evidence_literature NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion SIO_000772 20881942 NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion wasDerivedFrom befree-20140225 NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_assertion wasGeneratedBy ECO_0000203 NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP633863.RAnz7VVWZFh01KbqMabuZj7mwWXO1IJKHmyp_4WpDVP1c130_provenance.