Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_assertion> ?p ?o ?g. }
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- NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_assertion type Assertion NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_head.
- NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_assertion description "[Mutations in FGFR1/FGF8/PROKR2 contributed to 7.8% of our patients with CPHD/SOD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_provenance.
- NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_assertion evidence source_evidence_literature NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_provenance.
- NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_assertion SIO_000772 22319038 NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_provenance.
- NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_assertion wasDerivedFrom befree-20150227 NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_provenance.
- NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_assertion wasGeneratedBy ECO_0000203 NP969402.RAKdtsghzJVaDyjtmNr3vBJ5fWU--GeSNREvWQQaQbmR4130_provenance.