Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_assertion description "[This mutation was recently described in a family of Italian descent with CVT and Charcot-Marie-Tooth deformity HOXD10 gene mutations were not identified in any of the other families or sporadic patients with CVT, suggesting that genetic heterogeneity underlies this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_assertion evidence source_evidence_literature NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_assertion SIO_000772 16450407 NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_assertion wasDerivedFrom befree-20150227 NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_assertion wasGeneratedBy ECO_0000203 NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463290.RAXAB4DtAJEyJlkoHvGjpWVq66AOM8pXTbgX-W8DorJhQ130_provenance.