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- source_evidence_literature type ECO_0000212 NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_assertion wasGeneratedBy ECO_0000203 NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_assertion wasDerivedFrom befree-20150227 NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_assertion SIO_000772 23163601 NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_assertion evidence source_evidence_literature NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.
- NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632294.RAsbudogJ4Q3gvxEAt3ken1j4yYrf6jcV8vym_3XcDeWI130_provenance.