Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_assertion> ?p ?o ?g. }
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- NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_assertion type Assertion NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_head.
- NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_assertion description "[The results of karyotypic, clinical, and ERP investigations of this family suggest that the recently described genes DISC1 and DISC2, which are directly disrupted by the breakpoint on chromosome 1, may have a role in the development of a disease phenotype that includes schizophrenia as well as unipolar and bipolar affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_provenance.
- NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_assertion evidence source_evidence_literature NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_provenance.
- NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_assertion SIO_000772 11443544 NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_provenance.
- NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_assertion wasDerivedFrom befree-20150227 NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_provenance.
- NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_assertion wasGeneratedBy ECO_0000203 NP886709.RAv8KxJzS7i6N80j49lEJUZVhssUi3rqMQQuAK0VIo3SI130_provenance.