Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion wasGeneratedBy ECO_0000203 NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion wasDerivedFrom befree-20150227 NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion SIO_000772 12734540 NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion evidence source_evidence_literature NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.
- NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_assertion description "[Germline mutations in the RET proto-oncogene are responsible for the development of human hereditary diseases, including multiple endocrine neoplasia (MEN) type 2A and 2B, familial medullary thyroid carcinoma (FMTC), and Hirschsprung's disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670660.RAVDp4R585aBti7PH2n8qtfWX2Gj2SPjT68jcNcu1NGgk130_provenance.