Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_assertion description "[Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_assertion evidence source_evidence_literature NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_assertion SIO_000772 15965158 NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_assertion wasDerivedFrom befree-20140225 NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_assertion wasGeneratedBy ECO_0000203 NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP535255.RAW0C1rA9mHs97Bc1KyinzH0j2Jd7ApA2YE6kKLPyt0IM130_provenance.