Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_assertion wasGeneratedBy ECO_0000203 NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_assertion wasDerivedFrom befree-20150227 NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_assertion SIO_000772 22490426 NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_assertion evidence source_evidence_literature NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.
- NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_assertion description "[Pelizaeus-Merzbacher disease (PMD; MIM#312080) is a rare X-linked leukodystrophy presenting with motor developmental delay associated with spasticity and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631464.RAF-BC2jgnTIdS10wMZiNB_m_sTd3Bakkm-YLxjxXR_ZY130_provenance.