Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP471802.RA1UKdSLFM8jnUddOtlFtcBxxnXRxOtthlDcbrDtSirr4130_provenance.