Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_assertion wasGeneratedBy ECO_0000203 NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_assertion wasDerivedFrom gad-20130706 NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_assertion SIO_000772 15831156 NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_assertion evidence source_evidence_literature NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_assertion description "[The results of our study suggest that, in addition to prothrombotic mutations such as Factor V Leiden, single-nucleotide polymorphisms should be considered in all children with congenital cardiac malformations who develop thrombosis. Malformations of the]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.