Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_assertion description "[One of the boys with DMD, GK, and AHC is shown by pulsed-field-gel electrophoresis to have a deletion which has a proximal endpoint at least 500 kb distal from the pERT87 (DXS164) locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_assertion evidence source_evidence_literature NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_assertion SIO_000772 2837087 NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_assertion wasDerivedFrom befree-20150227 NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_assertion wasGeneratedBy ECO_0000203 NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355447.RAmtu1MkXyq90myVcJKFZ6QdgKltMELJXNwFUt2-Gx80w130_provenance.