Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_assertion description "[C.ommon prion protein gene (PRNP) codon 129 polymorphism is a strong susceptibility factor for human prion diseases/of methionine and valine may be a susceptibility factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_assertion evidence source_evidence_literature NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_assertion SIO_000772 18191917 NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_assertion wasDerivedFrom lhgdn-20090331 NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_assertion wasGeneratedBy ECO_0000203 NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP214052.RA3Tec4abzJiuvfZFptYGkdq1bOmtWgO9MN4PQlCqRrq8130_provenance.