Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_assertion description "[The autosomal-dominant axonal peripheral neuropathies comprise a genetically heterogeneous group of disorders that are clinically subsumed under Charcot-Marie-Tooth disease type 2 (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_assertion evidence source_evidence_literature NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_assertion SIO_000772 16775367 NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_assertion wasDerivedFrom befree-20140225 NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_assertion wasGeneratedBy ECO_0000203 NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP815643.RAZyIbN5bnfxXvf2ZpHDlWkiaFDNwi2aq0Mo3ionVNF6E130_provenance.