Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_assertion description "[Two siblings affected with a mild form of JS were found to have a homozygous deletion of the NPHP1 gene identical, by mapping, to that in subjects with NPHP alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_assertion evidence source_evidence_literature NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_assertion SIO_000772 15138899 NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_assertion wasDerivedFrom gad-20130706 NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_assertion wasGeneratedBy ECO_0000203 NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.