Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_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." NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_assertion evidence source_evidence_literature NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_assertion SIO_000772 8895241 NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_assertion wasDerivedFrom befree-20140225 NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_assertion wasGeneratedBy ECO_0000203 NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.