Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion evidence source_evidence_literature NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion SIO_000772 23304067 NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion wasDerivedFrom befree-20150227 NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion wasGeneratedBy ECO_0000203 NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.