Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_assertion description "[All NB susceptibility genes replicated in the Italian dataset except for DDX4 and IL31RA, and the most significant SNP was rs6435862 in BARD1 (P = 8.4 � 10(-15)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_assertion evidence source_evidence_literature NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_assertion SIO_000772 23222812 NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_assertion wasDerivedFrom befree-20150227 NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_assertion wasGeneratedBy ECO_0000203 NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP911913.RA7nlXO3wIklNl38P2jBe62QBA9yKcjCIEIshKKOMjamQ130_provenance.