Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_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." NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion evidence source_evidence_literature NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion SIO_000772 9595994 NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion wasDerivedFrom befree-20140225 NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion wasGeneratedBy ECO_0000203 NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.