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- source_evidence_literature type ECO_0000212 NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_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." NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_assertion evidence source_evidence_literature NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_assertion SIO_000772 12632326 NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_assertion wasDerivedFrom befree-2016 NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_assertion wasGeneratedBy ECO_0000203 NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.
- befree-2016 importedOn "2016-02-19" NP386784.RAWwNB8eS1FH5x1wXbsoV9e1A01HpikZNNU-bz5NNZkIw130_provenance.