Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_assertion evidence source_evidence_literature NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_assertion SIO_000772 19247433 NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_assertion wasDerivedFrom befree-20140225 NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_assertion wasGeneratedBy ECO_0000203 NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.