Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_assertion description "[Homozygous Pex10 mutant mouse embryos display biochemical abnormalities related to a PBD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_assertion evidence source_evidence_literature NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_assertion SIO_000772 25176044 NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_assertion wasDerivedFrom befree-20150227 NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_assertion wasGeneratedBy ECO_0000203 NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616335.RAktH5VaJYiy9K9FJWX-WKlIwR3RpxT2F__FHrCuLeoWI130_provenance.