Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_assertion description "[In this report, we describe two unrelated patients with mental retardation and brachydactyly E classified as patients suffering from Albright hereditary osteodystrophy-like (AHO-like) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_assertion evidence source_evidence_literature NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_assertion SIO_000772 15547662 NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_assertion wasDerivedFrom befree-20140225 NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_assertion wasGeneratedBy ECO_0000203 NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614975.RAcB0cRH78rkguuGJKysBHQ6IAxOglKx9LhJ7IasxElbI130_provenance.