Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion description "[Probands from each family were screened for mutations in 13 genes known to cause adRP: CA4, CRX, FSCN2, IMPDH1, NRL, PRPF3 (RP18), PRPF8 (RP13), PRPF31 (RP11), RDS, RHO, ROM1, RP1, and RP9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion evidence source_evidence_literature NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion SIO_000772 16799052 NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion wasDerivedFrom befree-20140225 NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_assertion wasGeneratedBy ECO_0000203 NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449061.RAzLChaggprJ6Ikul9BTEfsYaLXGc5NwyMXkdAklYRnQw130_provenance.