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- source_evidence_literature type ECO_0000212 NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_assertion description "[A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_assertion evidence source_evidence_literature NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_assertion SIO_000772 11280716 NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_assertion wasDerivedFrom befree-20150227 NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_assertion wasGeneratedBy ECO_0000203 NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.
- befree-20150227 importedOn "2015-02-27" NP571886.RAfPsPSgcpYlkbBuSceBdJXLY2B3VCVCI2ZDPE8Xq9iro130_provenance.