Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_assertion description "[DA type 5D (DA5D) is a rare, autosomal-recessive DA previously defined by us and is characterized by congenital contractures of the hands and feet, along with distinctive facial features, including ptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_assertion evidence source_evidence_literature NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_assertion SIO_000772 23261301 NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_assertion wasDerivedFrom befree-20140225 NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_assertion wasGeneratedBy ECO_0000203 NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.
- befree-20140225 importedOn "2014-02-25" NP576841.RAl7lhdC1FGe_Aj-jI-paFXk69UqoFVIrcBaN72fSw9Ug130_provenance.