Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_assertion wasGeneratedBy ECO_0000203 NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_assertion wasDerivedFrom befree-20150227 NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_assertion SIO_000772 14617022 NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_assertion evidence source_evidence_literature NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.
- NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_assertion description "[Lamin B-receptor mutations in Pelger-Huët anomaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532228.RACaKtkNAPMIW2m04_2ucQDqP8rzqaezFqnwnsRqwTxKc130_provenance.