Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_assertion description "[Four genes (NIPA1, NIPA2, CYFIP1, and GCP5) have been identified in the chromosomal region between breakpoints 1 and 2 and are implicated in compulsive behavior and lower intellectual ability observed in individuals with Prader-Willi syndrome with TI versus TII deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_assertion evidence source_evidence_literature NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_assertion SIO_000772 16982806 NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_assertion wasDerivedFrom befree-20140225 NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_assertion wasGeneratedBy ECO_0000203 NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.
- befree-20140225 importedOn "2014-02-25" NP355197.RAPJ1UScJAbrH7eeB-um3oBQGySX03t3mZoMhz7h2Tkas130_provenance.