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- NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_assertion type Assertion NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_head.
- NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_assertion wasGeneratedBy ECO_0000203 NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_provenance.
- NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_assertion wasDerivedFrom befree-20140225 NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_provenance.
- NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_assertion SIO_000772 23018678 NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_provenance.
- NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_assertion evidence source_evidence_literature NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_provenance.
- NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_assertion description "[Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925804.RAZkFysep0UdJO-1zr2C6ESMNfKR09VRcvoudvCEcJ-rg130_provenance.