Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_assertion description "[Myotilinopathies and desminopathies are subgroups of myofibrillar myopathies (MFM) caused by mutations in myotilin and desmin genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_assertion evidence source_evidence_literature NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_assertion SIO_000772 17784878 NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_assertion wasDerivedFrom befree-2016 NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_assertion wasGeneratedBy ECO_0000203 NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.
- befree-2016 importedOn "2016-02-19" NP628106.RAF2YDTVP26gLpR52bqk65dDvD5cgx8kDfUlJTmm2DhCs130_provenance.