Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_assertion description "[The study provides evidence that hypocretin deficiency causes a more severe NC phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_assertion evidence source_evidence_literature NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_assertion SIO_000772 20175400 NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_assertion wasDerivedFrom befree-2016 NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_assertion wasGeneratedBy ECO_0000203 NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.
- befree-2016 importedOn "2016-02-19" NP795194.RAABVFFSv7Z8ggAffM8ZUAvUhNxR3Ds77kJ1YYbhshqBo130_provenance.