Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_assertion description "[Acoustic function in the groups of various forms of ataxia with multiple system atrophy of cerebellar predominance (MSA-C), cortical cerebellar atrophy (CCA), and hereditary ataxias including SCA31 was evaluated by using audiogram and brainstem auditory evoked potentials (BAEPs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_assertion evidence source_evidence_literature NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_assertion SIO_000772 21535943 NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_assertion wasDerivedFrom befree-2016 NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_assertion wasGeneratedBy ECO_0000203 NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.
- befree-2016 importedOn "2016-02-19" NP891001.RA5LcIJ1hFBpNMWs7m_Yj_0vg0o6XKQlbgvKQYVTOSC3c130_provenance.