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- source_evidence_literature type ECO_0000212 NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_assertion description "[Recently, mutations in RPGRIP were found to lead to the retinal dystrophy, Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_assertion evidence source_evidence_literature NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_assertion SIO_000772 12140192 NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_assertion wasDerivedFrom befree-20140225 NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_assertion wasGeneratedBy ECO_0000203 NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP801772.RAVy-gpHeR7dXxRM0hiZ6Qwf0Xkj_JNRnGJwKQaX9p9gI130_provenance.