Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_assertion> ?p ?o ?g. }
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- NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_assertion type Assertion NP27455.RAJSk0i7gp9CrdFjxJzX_EpMyHXRJXRrB-bSUzaSuUlqA130_head.
- 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.