Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_assertion description "[These findings reveal several cellular defects in cells carrying the PHC1 mutation and highlight the role of chromatin remodeling in the pathogenesis of PM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_assertion evidence source_evidence_literature NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_assertion SIO_000772 23418308 NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_assertion wasDerivedFrom befree-20140225 NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_assertion wasGeneratedBy ECO_0000203 NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP937213.RALHE6fI6sNF6aZCtDMOnEfxNTtnsB4u3Vz66ueySq27w130_provenance.