Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_assertion wasGeneratedBy ECO_0000218 NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_assertion wasDerivedFrom ctd_human-20150221 NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_assertion SIO_000772 21091464 NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_assertion evidence source_evidence_curated NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.
- NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_assertion description "[Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_provenance.