Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_assertion evidence source_evidence_literature NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_assertion SIO_000772 16000300 NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_assertion wasDerivedFrom befree-20150227 NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_assertion wasGeneratedBy ECO_0000203 NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.