Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_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." NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_assertion evidence source_evidence_literature NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_assertion SIO_000772 2837087 NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_assertion wasDerivedFrom befree-20140225 NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_assertion wasGeneratedBy ECO_0000203 NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP298767.RA4xm471Z5G2eAiE493pfs_G7NlYMvDDSeEcjBSKi5Yyk130_provenance.