Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_assertion> ?p ?o ?g. }
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- NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_assertion type Assertion NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_head.
- NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_assertion description "[These results suggest that clinical manifestations in SHOC2 mutation-positive patients partially overlap with those in patients with typical Noonan or CFC syndrome and show that easily pluckable/loose anagen hair is distinctive in SHOC2 mutation-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_provenance.
- NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_assertion evidence source_evidence_literature NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_provenance.
- NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_assertion SIO_000772 20882035 NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_provenance.
- NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_assertion wasDerivedFrom befree-20140225 NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_provenance.
- NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_assertion wasGeneratedBy ECO_0000203 NP269744.RA4ijEnEoqa_Bd1towWnQKOiEpmdjRHDNSCsEoNMQ_y5w130_provenance.