Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_assertion> ?p ?o ?g. }
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- NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_assertion type Assertion NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_head.
- NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_assertion description "[We also believe that the deletion of GPR35 could be responsible for the entity brachydactyly mental retardation syndrome (OMIM #600430), which was coined based on the above minority of patients with terminal 2q37 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_provenance.
- NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_assertion evidence source_evidence_literature NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_provenance.
- NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_assertion SIO_000772 15521982 NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_provenance.
- NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_assertion wasDerivedFrom befree-2016 NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_provenance.
- NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_assertion wasGeneratedBy ECO_0000203 NP467153.RAuhpQ8RtB4SlmnuNKUI0aZ3dP0iZ8Fzc8jem8aR_OpPs130_provenance.