Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_assertion type Assertion NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_head.
- NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_assertion description "[In this study, we screened the entire coding region of FSHR gene for pathogenic mutations in women with premature ovarian failure (POF) (n = 16) and polycystic ovary syndrome (PCOS) (n = 124) and found no mutations in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_provenance.
- NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_assertion evidence source_evidence_literature NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_provenance.
- NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_assertion SIO_000772 11383926 NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_provenance.
- NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_assertion wasDerivedFrom befree-20140225 NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_provenance.
- NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_assertion wasGeneratedBy ECO_0000203 NP280966.RAIz80b0_n1WoHnhywVFklL6fkU5BydsW2R1FG8t_Dq14130_provenance.