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- NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_assertion type Assertion NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_head.
- 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.