Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion description "[This is the second report of LCA5 mutations causing Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion evidence source_evidence_literature NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion SIO_000772 18334959 NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion wasDerivedFrom lhgdn-20090331 NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion wasGeneratedBy ECO_0000203 NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.