Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_assertion description "[Germline mutations in RET are responsible for multiple endocrine neoplasia type 2 (MEN2), an autosomal dominantly inherited cancer syndrome that is characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and parathyroid hyperplasia/adenoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_assertion evidence source_evidence_literature NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_assertion SIO_000772 16707008 NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_assertion wasDerivedFrom befree-20140225 NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_assertion wasGeneratedBy ECO_0000203 NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.