Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_assertion description "[We sought somatic mutations in the corresponding genes in the CRCs of the patients harboring the germline lesions and found biallelic inactivation of FANCM, LAMB4, PTCHD3, LAMC3, and TREX2, potentially implicating these genes as tumor suppressors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_assertion evidence source_evidence_literature NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_assertion SIO_000772 23585368 NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_assertion wasDerivedFrom befree-20150227 NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_assertion wasGeneratedBy ECO_0000203 NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932954.RAdrdlHTNlqMwDrV7DpxJcU0GW1p6Rg1UVRu4DX1KiknE130_provenance.