Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_assertion description "[Although mutations in eight different genes (EDNRB, EDN3, ECE1, SOX10, RET, GDNF, NTN, SIP1) have been identified in affected individuals, it is now clear that RET and EDNRB are the primary genes implicated in the etiology of HSCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_assertion evidence source_evidence_literature NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_assertion SIO_000772 16618617 NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_assertion wasDerivedFrom befree-20150227 NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_assertion wasGeneratedBy ECO_0000203 NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP816536.RA8PhfyTSLWU33PetPpYHvcrwfV7nP7pJcnzjp7wI5Nkc130_provenance.