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- source_evidence_literature type ECO_0000212 NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_assertion description "[With the aim to conclusively validate the strongest associations so far reported, we selected the polymorphisms rs2227667 (SERPINE1), rs17501108 (HGF), rs3136685 (CCR7), rs16944 (IL1B), rs12147254 (TRAF3), rs1805087 (MTR), rs1800629 (TNF-?), rs7516435 (CASP9), rs1042265 (BAX), rs2234922 (mEH), and rs1801133 (MTHFR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_assertion evidence source_evidence_literature NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_assertion SIO_000772 24521996 NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_assertion wasDerivedFrom befree-20150227 NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_assertion wasGeneratedBy ECO_0000203 NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP607387.RAZw6P5V1BVQgBm1re5S6v2uPa0U1nNPlukZj6S2EHjJU130_provenance.