Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_assertion description "[MYH9-related disease ( MYH9-RD) is an autosomal dominant thrombocytopenia with giant platelets variably associated with young-adult onset of progressive sensorineural hearing loss, presenile cataract, and renal damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_assertion evidence source_evidence_literature NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_assertion SIO_000772 20174760 NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_assertion wasDerivedFrom befree-20140225 NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_assertion wasGeneratedBy ECO_0000203 NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.
- befree-20140225 importedOn "2014-02-25" NP767139.RAFKCXGtyA6hsxmyiXnapQetJ5IimAffHBy2BL8lEvCik130_provenance.