Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_assertion description "[We have studied patients with Duchenne muscular dystrophy (DMD), DMD together with glycerol kinase (GK) deficiency, or DMD together with both GK deficiency and congenital adrenal hypoplasia (AHC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_assertion evidence source_evidence_literature NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_assertion SIO_000772 2837087 NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_assertion wasDerivedFrom befree-20150227 NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_assertion wasGeneratedBy ECO_0000203 NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426729.RAyHYyEK_fztTW3WUHoSFn6hcXmIvR0i9t9rcOditdS2g130_provenance.