Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_assertion description "[Linkage to 1p35-p36 (CMT2A), 3q (CMT2B), and 7p (CMT2D) chromosomes has been reported in the disease; however, most HMSN II families do not link to any of the reported loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_assertion evidence source_evidence_literature NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_assertion SIO_000772 9595994 NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_assertion wasDerivedFrom befree-20150227 NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_assertion wasGeneratedBy ECO_0000203 NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP815664.RA0UxAl4dyI-n7XTNY1qeBUlb-uSSlvPEpfJuqAUOpORo130_provenance.