Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_assertion description "[Mutations in TBX3 that result in reduced functional protein lead to ulnar-mammary syndrome, a developmental disorder characterized by limb, mammary gland, tooth, and genital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_assertion evidence source_evidence_literature NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_assertion SIO_000772 22535523 NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_assertion wasDerivedFrom befree-20140225 NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_assertion wasGeneratedBy ECO_0000203 NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP692293.RA0EBoos0_sTomcnGrJAoCKE2ZFY5h1s6cIpduASL48BE130_provenance.