Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_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." NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_assertion evidence source_evidence_literature NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_assertion SIO_000772 16618617 NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_assertion wasDerivedFrom befree-20150227 NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_assertion wasGeneratedBy ECO_0000203 NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP599209.RAbqkujsvAVtgNzojRWE1SmFLhEKCQCYMA19Go_dWu0Lw130_provenance.