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- source_evidence_literature type ECO_0000212 NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_assertion description "[A novel RUNX2 missense mutation has been found in members of a family clinically diagnosed with cleidocranial dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_assertion evidence source_evidence_literature NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_assertion SIO_000772 16244783 NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_assertion wasDerivedFrom lhgdn-20090331 NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_assertion wasGeneratedBy ECO_0000203 NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP216834.RABJ00hO6xuyXKYyhJulPC_N93N0p_x25UuzPRbcK5mfU130_provenance.