Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_assertion description "[Mutations in the alpha-skeletal actin gene (ACTA1) result in a variety of inherited muscle disorders characterized by different pathologies and variable clinical phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_assertion evidence source_evidence_literature NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_assertion SIO_000772 17705262 NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_assertion wasDerivedFrom befree-20140225 NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_assertion wasGeneratedBy ECO_0000203 NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP839180.RAOG5vgWJuw95Ag1O9-a0BRlUVtnMxLSIJoasRWuku-PE130_provenance.