Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_assertion description "[The most common form of HSP is caused by mutations of the spastin gene (SPAST), located on chromosome 2p21-p22, which encodes spastin, one of the ATPases associated with diverse cellular activities (AAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_assertion evidence source_evidence_literature NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_assertion SIO_000772 16788734 NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_assertion wasDerivedFrom befree-20140225 NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_assertion wasGeneratedBy ECO_0000203 NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP513777.RA3CNwd-gPKw8GuNz_BHWaM8z4tbfBNoIPh34eOyizxyo130_provenance.