Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_assertion wasGeneratedBy ECO_0000203 NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_assertion wasDerivedFrom befree-20140225 NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_assertion SIO_000772 20844025 NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_assertion evidence source_evidence_literature NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_assertion description "[We studied an adult patient with ORD due to homozygous POR A287P, the most frequent POR mutation in Caucasians, and her clinically unaffected, heterozygous mother.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP746716.RArFiDd_9Iw_c-iNXcYhb4gAjacd-eJPYWLv-MyfhuLVM130_provenance.