Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_assertion description "[In this paper, we describe a boy with a 46,Y,der(X)t(X;Y)(p22.3;q11)mat karyotype and review the genotype-phenotype correlations in three male patients with the combination of apparent lack of clinical features of CDPX1 and a partial deletion of the critical region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_assertion evidence source_evidence_literature NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_assertion SIO_000772 7759082 NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_assertion wasDerivedFrom befree-20140225 NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_assertion wasGeneratedBy ECO_0000203 NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP368309.RA2dQJ3jzXnE3pfNBe7ZABROUxbD7UZaW1lGOK1mv2y-o130_provenance.