Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion> ?p ?o ?g. }
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- NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion type Assertion NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_head.
- NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_provenance.
- NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion evidence source_evidence_literature NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_provenance.
- NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion SIO_000772 10644430 NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_provenance.
- NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion wasDerivedFrom befree-20140225 NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_provenance.
- NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_assertion wasGeneratedBy ECO_0000203 NP880741.RAb5IcPMO_D82IbEKn_qqoss4NyiCE_KWBMJWZOZ3cJt4130_provenance.