Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_assertion wasGeneratedBy ECO_0000203 NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_assertion wasDerivedFrom lhgdn-20090331 NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_assertion SIO_000772 12467726 NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_assertion evidence source_evidence_literature NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.
- NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_assertion description "[Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the CMD1B locus in three Tunisian patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189963.RAzYSD3m7BsKPqBZN4F2NnMdgklEUTkJ_U9YRtiy1dt3g130_provenance.