Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_assertion description "[Restricting the analysis to the subset of families (n=49) with two or more individuals having a narrow diagnosis of autism and PSD generated a maximal multipoint HLOD score of 2.99 and an NPL score of 3.32.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_assertion evidence source_evidence_literature NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_assertion SIO_000772 11353400 NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_assertion wasDerivedFrom befree-2016 NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_assertion wasGeneratedBy ECO_0000203 NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP317924.RAXnG1TEmJhHlIDWXsILK95GOV6uvrSZ1C3uciiwjqxR0130_provenance.