Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion description "[The Pro56Ser mutation in the human VAPB MSP domain causes a familial amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion evidence source_evidence_literature NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion SIO_000772 20377183 NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion wasDerivedFrom befree-20150227 NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion wasGeneratedBy ECO_0000203 NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.