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- source_evidence_literature type ECO_0000212 NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_assertion description "[Thus, we tested the hypothesis that a mutation within MYH9 is responsible for the autosomal dominant inheritance of MTCP and hearing loss in the Ghent family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_assertion evidence source_evidence_literature NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_assertion SIO_000772 19285578 NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_assertion wasDerivedFrom befree-20150227 NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_assertion wasGeneratedBy ECO_0000203 NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.