Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_assertion description "[FHL1 mutations cause Emery-Dreifuss muscular dystrophy (OMIM 310300), X-linked myopathy with postural muscle atrophy (XMPMA, OMIM 300696), scapuloperoneal myopathy (OMIM 300695), or reducing body myopathy (OMIM 300717, 300718).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_assertion evidence source_evidence_literature NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_assertion SIO_000772 21932316 NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_assertion wasDerivedFrom befree-20150227 NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_assertion wasGeneratedBy ECO_0000203 NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.
- befree-20150227 importedOn "2015-02-27" NP403600.RAC4v3YqNGMncDDFnax-Su854E4RM9Zsgrf-xzTQ642Go130_provenance.