Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_assertion description "[The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_assertion evidence source_evidence_literature NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_assertion SIO_000772 11106354 NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_assertion wasDerivedFrom befree-20150227 NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_assertion wasGeneratedBy ECO_0000203 NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936009.RALZT4bWPENamOrxS8ohtRNWfuFQsrgzWtGBXcGuS-lco130_provenance.