Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_assertion description "[A unique micro-deletion including this enhancer element, but not the DLX5/DLX6 genes, was identified in a patient with SHFM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_assertion evidence source_evidence_literature NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_assertion SIO_000772 20808887 NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_assertion wasDerivedFrom befree-20140225 NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_assertion wasGeneratedBy ECO_0000203 NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404807.RAFd0nmHxLVBlSSHPu41JoUB04hFrkKhpVaW3ONgNj_zI130_provenance.