Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion> ?p ?o ?g. }
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- NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_assertion type Assertion NP585962.RASLFHFgH2Vk1zVoQSDDPHTCWBzLeXBv_UI6XtP6wusvw130_head.
- 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.