Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_assertion description "[study tested for the association of four SNPs of NPTX2 & haplotypes consisting of the SNPs with autism, between autistic patients & controls in a Japanese population; no significant difference was observed in allele, genotype or haplotype frequencies ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_assertion evidence source_evidence_literature NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_assertion SIO_000772 17408830 NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_assertion wasDerivedFrom lhgdn-20090331 NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_assertion wasGeneratedBy ECO_0000203 NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134651.RAkzWrgXFtQpHbmd4jkxyQCxm772C33lthoIPOQ1zYFQE130_provenance.