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- source_evidence_literature type ECO_0000212 NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_assertion description "[LIPH is a second causative gene for ARWH/hypotrichosis, giving rise to a phenotype clinically indistinguishable from P2RY5 mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_assertion evidence source_evidence_literature NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_assertion SIO_000772 18830268 NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_assertion wasDerivedFrom lhgdn-20090331 NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_assertion wasGeneratedBy ECO_0000203 NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP242539.RAfSptSV-F4rdW0K0WAns98i70Ubr4G9bt1ZT8SQJZK6o130_provenance.