Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_assertion description "[Mutations in the skeletal muscle gene dysferlin cause two autosomal recessive forms of muscular dystrophy: Miyoshi myopathy (MM) and limb girdle muscular dystrophy type 2B (LGMD2B).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_assertion evidence source_evidence_literature NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_assertion SIO_000772 11468312 NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_assertion wasDerivedFrom befree-2016 NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_assertion wasGeneratedBy ECO_0000203 NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.
- befree-2016 importedOn "2016-02-19" NP324898.RA4GB9nyuq7nXmTMdvPmn65ckyCb3ejd3KD33KqNyd6W0130_provenance.