Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_assertion> ?p ?o ?g. }
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- NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_assertion type Assertion NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_head.
- NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_assertion description "[PROP1 mutations are rare in sporadic cases of CPHD, although the prevalence rises if there is a positive family history or if the patients are carefully selected with respect to the endocrine and neuroradiological phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_provenance.
- NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_assertion evidence source_evidence_literature NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_provenance.
- NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_assertion SIO_000772 15963055 NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_provenance.
- NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_assertion wasDerivedFrom befree-20140225 NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_provenance.
- NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_assertion wasGeneratedBy ECO_0000203 NP413158.RA5ElQrLJS0XEfFrY9Wu7ohhZpxmwtcaRp_RCU00XpZPc130_provenance.