Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_assertion description "[Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_assertion evidence source_evidence_literature NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_assertion SIO_000772 20493457 NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_assertion wasDerivedFrom befree-20150227 NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_assertion wasGeneratedBy ECO_0000203 NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP711763.RA4HiMWOb0RGVvy6ph6kUCdX-TU6FIAVvJ3kPCs9A8ETU130_provenance.