Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_assertion description "[Rare, potentially deleterious HOMER1 variants identified uniquely in the autism population affected functionally important protein regions or regulatory sequences and co-segregated closely with autism among children of affected families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_assertion evidence source_evidence_literature NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_assertion SIO_000772 22558107 NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_assertion wasDerivedFrom befree-20150227 NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_assertion wasGeneratedBy ECO_0000203 NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824168.RAJYc8Fw-FhIv4Ld5ExRNqnwHKkku2IUZTeh9VQt-AJNY130_provenance.