Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_assertion description "[SHANK3 mutations have also been reported in autistic patients without a syndromic phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_assertion evidence source_evidence_literature NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_assertion SIO_000772 21271662 NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_assertion wasDerivedFrom befree-20140225 NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_assertion wasGeneratedBy ECO_0000203 NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP576138.RA2qwKph3PsCVxnDwT3qafhY8Q2XT_yy4XoWYAszA_Irk130_provenance.