Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion description "[There is a remarkable degree of clinical variability both within and between families with Marfan syndrome as well as in individuals with related disorders of connective tissue caused by FBN1 mutations and collectively termed type-1 fibrillinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion evidence source_evidence_literature NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion SIO_000772 11175294 NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion wasDerivedFrom befree-2016 NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_assertion wasGeneratedBy ECO_0000203 NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.
- befree-2016 importedOn "2016-02-19" NP307095.RARbcdQqoy7VRODCtHNxCPudSK9OePIe1_Li-B3KXil40130_provenance.