Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_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." NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion evidence source_evidence_literature NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion SIO_000772 24877152 NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion wasDerivedFrom befree-20150227 NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion wasGeneratedBy ECO_0000203 NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.