Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion evidence source_evidence_literature NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion SIO_000772 11835375 NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion wasDerivedFrom befree-20140225 NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion wasGeneratedBy ECO_0000203 NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_provenance.