Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_assertion> ?p ?o ?g. }
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- NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_assertion type Assertion NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_head.
- NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_assertion description "[Therefore, we tested the hypothesis that ATP1A2 mutations in patients with FHM-2 are associated with hypersensitivity to NO-cGMP pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.
- NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_assertion evidence source_evidence_literature NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.
- NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_assertion SIO_000772 18294248 NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.
- NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_assertion wasDerivedFrom befree-20140225 NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.
- NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_assertion wasGeneratedBy ECO_0000203 NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.