Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_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." NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_assertion evidence source_evidence_literature NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_assertion SIO_000772 16788734 NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_assertion wasDerivedFrom befree-20140225 NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_assertion wasGeneratedBy ECO_0000203 NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP879913.RAntNRwpb6VDkBVCT1gw5J-iEkdLvzf_oxbyZcosRtI8E130_provenance.