Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_assertion description "[In human muscle, fibrosis is most readily associated with the severe muscle wasting disorder Duchenne muscular dystrophy (DMD), caused by loss of dystrophin gene function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_assertion evidence source_evidence_literature NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_assertion SIO_000772 24877152 NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_assertion wasDerivedFrom befree-2016 NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_assertion wasGeneratedBy ECO_0000203 NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1186827.RAS2cg006qWsVO_oQOxgoV6r-_SUgyfwFzQTnPv2CmfXw130_provenance.