Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion type Assertion NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_head.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion wasGeneratedBy ECO_0000203 NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion wasDerivedFrom befree-20140225 NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion SIO_000772 11297579 NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion evidence source_evidence_literature NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion description "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.