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- source_evidence_literature type ECO_0000212 NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_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." NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_assertion evidence source_evidence_literature NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_assertion SIO_000772 12632326 NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_assertion wasDerivedFrom befree-20150227 NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_assertion wasGeneratedBy ECO_0000203 NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP941688.RA59XtdQZgi1egtbjznIUXBj6PA7e9qbGmhsAw49b427s130_provenance.