Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_assertion wasGeneratedBy ECO_0000203 NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_assertion wasDerivedFrom befree-20140225 NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_assertion SIO_000772 22452838 NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_assertion evidence source_evidence_literature NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_assertion description "[PCH is most often autosomal recessive though de novo anomalies in the X-linked gene CASK have recently been identified in patients, mostly females, presenting with intellectual disability, microcephaly and PCH (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.