Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_assertion> ?p ?o ?g. }
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- NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_assertion type Assertion NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_head.
- NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_assertion wasGeneratedBy ECO_0000218 NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_provenance.
- NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_assertion wasDerivedFrom ctd_human-20130708 NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_provenance.
- NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_assertion SIO_000772 15146389 NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_provenance.
- NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_assertion evidence source_evidence_curated NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_provenance.
- NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_assertion description "[A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18286.RAQuVw5F9Oc3834A679EshCWtTZ6f2AUlegu9n3xGfcp0130_provenance.