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- source_evidence_literature type ECO_0000212 NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_assertion description "[The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_assertion evidence source_evidence_literature NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_assertion SIO_000772 16076902 NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_assertion wasDerivedFrom befree-20150227 NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_assertion wasGeneratedBy ECO_0000203 NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP848986.RAMnhPbc3P5USfiL_z_gSPR9638-PejGvhHshFNw3fnPQ130_provenance.