Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_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." NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_assertion evidence source_evidence_literature NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_assertion SIO_000772 7683951 NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_assertion wasDerivedFrom befree-20140225 NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_assertion wasGeneratedBy ECO_0000203 NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681522.RABnsTRu65_8NM32UuaTI8ERclNvLaq-MVt_b5qhDqAKA130_provenance.