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- source_evidence_literature type ECO_0000212 NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_assertion description "[OCA type 2 (OCA2), the most common form of OCA, is an autosomal recessive disorder caused by mutations in the P gene, the function(s) of which is controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_assertion evidence source_evidence_literature NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_assertion SIO_000772 12028586 NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_assertion wasDerivedFrom befree-2016 NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_assertion wasGeneratedBy ECO_0000203 NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.
- befree-2016 importedOn "2016-02-19" NP355809.RA4PdopcfNwtRnn03dfX7zH4E5yoF0mHxgorJ6iAuOKqA130_provenance.