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- source_evidence_literature type ECO_0000212 NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion description "[The contribution of copy number variation (CNV) to specific congenital heart disease (CHD) phenotypes including AVSD is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion evidence source_evidence_literature NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion SIO_000772 22529060 NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion wasDerivedFrom befree-20150227 NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion wasGeneratedBy ECO_0000203 NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.