Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_assertion evidence source_evidence_literature NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_assertion SIO_000772 15174025 NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_assertion wasDerivedFrom befree-20150227 NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_assertion wasGeneratedBy ECO_0000203 NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.