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- source_evidence_literature type ECO_0000212 NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_assertion description "[No associations were found with the AR (GGC)(n), CYP17 Msp A1 I, VDR Taq I, SRD5A2 (TA)(n) and p.49A >T polymorphisms and CaP risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_assertion evidence source_evidence_literature NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_assertion SIO_000772 15711606 NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_assertion wasDerivedFrom befree-2016 NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_assertion wasGeneratedBy ECO_0000203 NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.
- befree-2016 importedOn "2016-02-19" NP480926.RA-dHxeN2rauscEsjtredpzJEH-A7b1qJNtfcuLenPQgw130_provenance.