Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_assertion> ?p ?o ?g. }
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- NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_assertion type Assertion NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_head.
- NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_assertion wasGeneratedBy ECO_0000203 NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_provenance.
- NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_assertion wasDerivedFrom befree-2016 NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_provenance.
- NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_assertion SIO_000772 16511839 NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_provenance.
- NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_assertion evidence source_evidence_literature NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_provenance.
- NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_assertion description "[Caused by a microdeletion at the q11.2 locus of chromosome 22, velo-cardio-facial syndrome (also known as VCFS, 22q11 deletion syndrome, DiGeorge sequence, and conotruncal anomalies face syndrome) is associated with a distinctive physical, neurocognitive, and psychiatric phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538427.RA7fbgpLd-G95OD5O_LvE9wTElYTeVHysGD658VKzVg2M130_provenance.