Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- befree-2016 importedOn "2016-02-19" NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_assertion wasGeneratedBy ECO_0000203 NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_assertion wasDerivedFrom befree-2016 NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_assertion SIO_000772 17164413 NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_assertion evidence source_evidence_literature NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.
- NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_assertion description "[Moreover, we show that transcription of Dlx3 is abrogated by mutations in the sterile alpha-motif (SAM) domain of p63 that are associated with ankyloblepharon-ectodermal dysplasia-clefting (AEC) dysplasias, but not by mutations found in ectrodactylyectodermal dysplasia-cleft lip/palate (EEC), Limb-mammary syndrome (LMS) and split hand-foot malformation (SHFM) dysplasias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583996.RAWEw5R40VSMg00dhVX6vsQI-oKnLWQtJ4VkCwxDM49-U130_provenance.