Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_assertion wasGeneratedBy ECO_0000203 NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_assertion wasDerivedFrom befree-2016 NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_assertion SIO_000772 8530067 NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_assertion evidence source_evidence_literature NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.
- NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_assertion description "[A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1344394.RA5Z4iUGIvL5E6f1WNgg1Zx35znRXztF-mQK7QCqQ4W6g130_provenance.