Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_assertion wasGeneratedBy ECO_0000203 NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_assertion wasDerivedFrom befree-20140225 NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_assertion SIO_000772 19932620 NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_assertion evidence source_evidence_literature NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_assertion description "[Centronuclear myopathy with cataracts due to a novel dynamin 2 (DNM2) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP871391.RAvX1FMCvsSv3Xj8AKCEG9y9TNr-xjdvLtpboU07N6ZPY130_provenance.