Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_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." NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_assertion evidence source_evidence_literature NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_assertion SIO_000772 8895241 NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_assertion wasDerivedFrom befree-20150227 NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_assertion wasGeneratedBy ECO_0000203 NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.