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- source_evidence_literature type ECO_0000212 NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_assertion description "[the first description of a mutation in cytoskeletal, or nonmuscle, actin; with an autosomal dominant, progressive, sensorineural hearing loss phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_assertion evidence source_evidence_literature NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_assertion SIO_000772 13680526 NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_assertion wasDerivedFrom lhgdn-20090331 NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_assertion wasGeneratedBy ECO_0000203 NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP201460.RAyEwKlWc3VCIs0BR2Zo8AIIHMRmJPQP7-tyEcNajMrf8130_provenance.