Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_assertion description "[We investigated the proteolipid protein (PLP) gene of two boys in a Japanese family with Pelizaeus-Merzbacher disease (PMD), an X-linked neurologic disorder characterized by dysmyelination in the central nervous system (CNS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_assertion evidence source_evidence_literature NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_assertion SIO_000772 7683951 NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_assertion wasDerivedFrom befree-2016 NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_assertion wasGeneratedBy ECO_0000203 NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1318068.RAhy3l2SojoFo0MMd3uA30v1BEXtjALpxc07Zbf9ceu6o130_provenance.