Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_assertion description "[We assessed the frequency of SDHB, SDHC, and SDHD gene mutations by PCR amplification and sequencing in a set of head and neck paraganglioma patients who were previously managed in two otolaryngology clinics in the USA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_assertion evidence source_evidence_literature NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_assertion SIO_000772 11897817 NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_assertion wasDerivedFrom gad-20130706 NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_assertion wasGeneratedBy ECO_0000203 NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52081.RAxDE-PmrqmOORxbV-m1J5bd3dO1kf29FYwJwT2vp1mcs130_provenance.