Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_assertion description "[Autosomal dominant spastic paraplegia, type 4 (SPG4), a debilitating disorder of progressive spasticity and weakness of the lower limbs, results from heterozygous mutations in the SPAST gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_assertion evidence source_evidence_literature NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_assertion SIO_000772 21659953 NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_assertion wasDerivedFrom befree-20150227 NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_assertion wasGeneratedBy ECO_0000203 NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710078.RAeW1IOC9lE75UxgsKorOqyZCjP93ZYyFEANguC5nEIIo130_provenance.