Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_assertion description "[The three-dimensional solution structure of the p63 sterile alpha-motif (SAM) domain (residues 505-579), a region crucial to explaining the human genetic disease ankyloblepharonectodermal dysplasia-clefting syndrome (AEC), has been determined by nuclear magnetic resonance spectroscopy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_assertion evidence source_evidence_literature NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_assertion SIO_000772 16679535 NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_assertion wasDerivedFrom befree-20140225 NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_assertion wasGeneratedBy ECO_0000203 NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889307.RAh913WWvSFSTMwiIJSVUgCmzjwFJNaL-4XZEq0Imd0Yc130_provenance.