Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_assertion description "[Absence of TNX mRNA and protein in the proband, mapping of the TNX gene and HLA typing of this family suggest recessive inheritance of TNX deficiency and connective-tissue disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_assertion evidence source_evidence_literature NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_assertion SIO_000772 9288108 NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_assertion wasDerivedFrom befree-20150227 NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_assertion wasGeneratedBy ECO_0000203 NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748913.RA41LngquJ0-QUDL4M6gih_KhcghiVnfH2u7wWUYd4vOI130_provenance.