Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_assertion description "[Beside point mutations, FSHR gene polymorphisms at specific sites (e.g., codons 307 and 680) may influence FSHR protein responsiveness to exogenous FSH, and finally affect the effectiveness of in vitro fertilization (IVF) treatment as well as the likelihood of developing a severe OHSS as a consequence of superovulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_assertion evidence source_evidence_literature NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_assertion SIO_000772 19017414 NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_assertion wasDerivedFrom befree-20150227 NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_assertion wasGeneratedBy ECO_0000203 NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673379.RA3Kk74Af2_gpPluPLmHPwLLpevzaltcV8gNZ1cWiIcoc130_provenance.