Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_assertion description "[VCP mutations in familial and sporadic amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_assertion evidence source_evidence_literature NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_assertion SIO_000772 22078486 NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_assertion wasDerivedFrom befree-20140225 NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_assertion wasGeneratedBy ECO_0000203 NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP848673.RAzvL6CKgMtC4ybHujOqwzDXNtJZCSsLG-L20bjsoXsDI130_provenance.