Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_assertion description "[Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_assertion evidence source_evidence_literature NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_assertion SIO_000772 17655765 NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_assertion wasDerivedFrom befree-20140225 NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_assertion wasGeneratedBy ECO_0000203 NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP300385.RAW3S5-wsS8D996XYFm_z5WnVb9SPiawW45HxOO4mistc130_provenance.