Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_assertion description "[This study confirms that the frequency of ARX mutations is high in XLMR, and the analysis of ARX in MRX should not be limited to duplication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_assertion evidence source_evidence_literature NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_assertion SIO_000772 16235064 NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_assertion wasDerivedFrom befree-20150227 NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_assertion wasGeneratedBy ECO_0000203 NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835544.RAi39jlGJFWoBY3Cq9ElNoh55bN7KmLC19ZxYTm2Ig29c130_provenance.