Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_assertion description "[Mutations in the ARX gene, at Xp22.3, cause several disorders, including infantile spasms, X-linked lissencephaly with abnormal genitalia (XLAG), callosal agenesis and isolated intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_assertion evidence source_evidence_literature NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_assertion SIO_000772 22585566 NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_assertion wasDerivedFrom befree-20150227 NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_assertion wasGeneratedBy ECO_0000203 NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835571.RAL50lvp8d5STy4z0qL_McX64QvqQHSo-DoM83F-680aU130_provenance.