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- NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_assertion type Assertion NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_head.
- NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_assertion description "[These results indicated that the polymorphism -9C>T and 368A>G in H2BFWT gene are associated with male infertility with idiopathic azoospermia or oligozoospermia, suggesting that H2BFWT gene might be contribute to susceptibility to spermatogenesis impairment in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_provenance.
- NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_assertion evidence source_evidence_literature NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_provenance.
- NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_assertion SIO_000772 22509975 NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_provenance.
- NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_assertion wasDerivedFrom befree-2016 NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_provenance.
- NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_assertion wasGeneratedBy ECO_0000203 NP975491.RAIm9y82se3Mttocyv-SsfB-Upggf2cxF07NxusOrxL9s130_provenance.