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- NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_assertion type Assertion NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_head.
- NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_assertion description "[A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_provenance.
- NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_assertion evidence source_evidence_curated NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_provenance.
- NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_assertion SIO_000772 9152842 NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_provenance.
- NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_assertion wasDerivedFrom uniprot-2016 NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_provenance.
- NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_assertion wasGeneratedBy ECO_0000218 NP9381.RAv5o4ncJMd9y2Zswtle1Kyc5qg78F_AAGPVD7SecM_ro130_provenance.