Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_assertion description "[Mutations in the p63 gene have been identified in five human disorders characterized by varying degrees of limb anomalies, ectodermal dysplasia, and facial clefts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_assertion evidence source_evidence_literature NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_assertion SIO_000772 16190990 NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_assertion wasDerivedFrom befree-20140225 NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_assertion wasGeneratedBy ECO_0000203 NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.
- befree-20140225 importedOn "2014-02-25" NP757598.RAQ0OX807gv_9padHbU7aSud-CvPeU_e4W0nI-iPQ3zas130_provenance.