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- source_evidence_literature type ECO_0000212 NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_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." NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_assertion evidence source_evidence_literature NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_assertion SIO_000772 7683951 NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_assertion wasDerivedFrom befree-20150227 NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_assertion wasGeneratedBy ECO_0000203 NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP658872.RA1cmCLCkfZYK5IwcEk-rdnIuy6NW8Itvgi6roSYguT_c130_provenance.