Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion> ?p ?o ?g. }
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- NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion type Assertion NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_head.
- NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion description "[Given that there are other eight MRX families overlapping this interval, none of them with known mutation, we conclude that at least one new gene responsible for nonsyndromic mental retardation is located in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance.
- NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion evidence source_evidence_literature NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance.
- NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion SIO_000772 15526294 NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance.
- NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion wasDerivedFrom befree-20140225 NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance.
- NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_assertion wasGeneratedBy ECO_0000203 NP475653.RAVowSMNI4vO4QvWQ5oeFuSzqNJLCnfILMkzrRQ_xMFaA130_provenance.