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- source_evidence_literature type ECO_0000212 NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_assertion evidence source_evidence_literature NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_assertion SIO_000772 18723471 NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_assertion wasDerivedFrom befree-2016 NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_assertion wasGeneratedBy ECO_0000203 NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.
- befree-2016 importedOn "2016-02-19" NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.