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- source_evidence_literature type ECO_0000212 NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_assertion description "[MYH9-associated disorders (May-Hegglin anomaly, Epstein and Fechtner syndrome, and others) are inherited in an autosomal dominant manner and characterized by defects in different organs (including eyes, ears, kidneys and thrombocytes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_assertion evidence source_evidence_literature NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_assertion SIO_000772 23144074 NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_assertion wasDerivedFrom befree-20150227 NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_assertion wasGeneratedBy ECO_0000203 NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583675.RAE8qUVD1agK6NWpqqtKhEsZFWpTm0ZBewqaAFSeWhksk130_provenance.