Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion description "[CRELD1 is the first human gene to be implicated in the pathogenesis of isolated AVSD and AVSD in the context of heterotaxy, which provides an important step in unraveling the pathogenesis of AVSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion evidence source_evidence_literature NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion SIO_000772 12632326 NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion wasDerivedFrom befree-20140225 NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion wasGeneratedBy ECO_0000203 NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance.