Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- befree-2016 importedOn "2016-02-19" NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_assertion wasGeneratedBy ECO_0000203 NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_assertion wasDerivedFrom befree-2016 NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_assertion SIO_000772 14966171 NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_assertion evidence source_evidence_literature NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.
- NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_assertion description "[MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431886.RAtXgMtbVkjT7rPkBQ5LeC5u0yXY9-KysmoLSm9iRFxi4130_provenance.