Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_assertion description "[One form of CMT2 maps to chromosome 1p36 (CMT2A), another to chromosome 3p (CMT2B) and another to 7p (CMT2D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_assertion evidence source_evidence_literature NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_assertion SIO_000772 10219749 NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_assertion wasDerivedFrom befree-20140225 NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_assertion wasGeneratedBy ECO_0000203 NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP333771.RA8mnSUmV-EJuCnq69hD66jMnU2__RK-VeP0uOwHkfBjc130_provenance.