Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_assertion description "[Mutations in the ARX gene are responsible for a wide variety of mental retardation conditions including X-linked infantile spasms (ISSX) and generalized dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_assertion evidence source_evidence_literature NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_assertion SIO_000772 18468866 NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_assertion wasDerivedFrom befree-20140225 NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_assertion wasGeneratedBy ECO_0000203 NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP837345.RAmdohXsCMTBqVA52wzCZ2alY0jGS_CPQG5qVUNnC5XZI130_provenance.