Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_assertion evidence source_evidence_literature NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_assertion SIO_000772 10320095 NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_assertion wasDerivedFrom befree-20150227 NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_assertion wasGeneratedBy ECO_0000203 NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP609392.RA2AvCEvA__ABJQA42V6zDw5FzVcGJZAHltPqBbhhkmCQ130_provenance.