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- source_evidence_literature type ECO_0000212 NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_assertion description "[The authors found that using both exome sequencing and allele frequency data from large sequencing efforts may aid genetic diagnosis of MH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_assertion evidence source_evidence_literature NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_assertion SIO_000772 24013571 NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_assertion wasDerivedFrom befree-2016 NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_assertion wasGeneratedBy ECO_0000203 NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108434.RAV5syRi_1yIw8p9ea2Cc13vRplWweOztupO4L1aWv0dA130_provenance.