Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_assertion> ?p ?o ?g. }
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- NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_assertion type Assertion NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_head.
- NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_assertion wasGeneratedBy ECO_0000203 NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_provenance.
- NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_assertion wasDerivedFrom befree-20150227 NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_provenance.
- NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_assertion SIO_000772 21091464 NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_provenance.
- NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_assertion evidence source_evidence_literature NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_provenance.
- NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_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." NP972784.RAD6xWM2YlLm3L1FAIxqHeRXYkTPOaPYwyEFf5iF9V7pw130_provenance.