Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_assertion evidence source_evidence_literature NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_assertion SIO_000772 8895241 NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_assertion wasDerivedFrom befree-20140225 NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_assertion wasGeneratedBy ECO_0000203 NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.