Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_assertion description "[We recently showed that some patients without MLC1 mutations display the classical phenotype; others improve or become normal but retain macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_assertion evidence source_evidence_literature NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_assertion SIO_000772 21419380 NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_assertion wasDerivedFrom befree-20150227 NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_assertion wasGeneratedBy ECO_0000203 NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP869890.RAsSj9-Cl7teR_ltnGoeM1VdtVtJ1ezkedV4DuVViE2rI130_provenance.