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- source_evidence_literature type ECO_0000212 NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_assertion description "[The results suggest that the PRNP variant allele at codon 171 (Asn171Ser) is associated with epileptogenesis in MTLE-HS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_assertion evidence source_evidence_literature NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_assertion SIO_000772 14610121 NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_assertion wasDerivedFrom befree-20140225 NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_assertion wasGeneratedBy ECO_0000203 NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP480973.RA_KawpNpwnVuwq6njGm_71Ni78IY0DtpONNNrBN62nW8130_provenance.