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- source_evidence_literature type ECO_0000212 NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_assertion description "[Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_assertion evidence source_evidence_literature NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_assertion SIO_000772 7649472 NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_assertion wasDerivedFrom befree-2016 NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_assertion wasGeneratedBy ECO_0000203 NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.